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Titolo:
Co-operation between human CR1 (CD35) and CR2 (CD21) in internalization oftheir C3b and iC3b ligands by murine-transfected fibroblasts
Autore:
Grattone, ML; Villiers, CL; Villiers, MB; Drouet, C; Marche, PN;
Indirizzi:
Univ Grenoble 1, INSERM, U238, DBMS ICH,CEAG, F-38054 Grenoble 9, France Univ Grenoble 1 Grenoble France 9 S ICH,CEAG, F-38054 Grenoble 9, France
Titolo Testata:
IMMUNOLOGY
fascicolo: 1, volume: 98, anno: 1999,
pagine: 152 - 157
SICI:
0019-2805(199909)98:1<152:CBHC(A>2.0.ZU;2-5
Fonte:
ISI
Lingua:
ENG
Soggetto:
T-DEPENDENT ANTIGEN; COMPLEMENT FACTOR-H; B-CELL RESPONSE; FACTOR-I; BINDING-SITES; TETANUS TOXIN; RECEPTOR; EXPRESSION; CR-2; COMPONENTS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
29
Recensione:
Indirizzi per estratti:
Indirizzo: Marche, PN Univ Grenoble 1, INSERM, U238, DBMS ICH,CEAG, 17 Rue Martyrs, F-38054 Grenoble 9, France Univ Grenoble 1 17 Rue Martyrs Grenoble France 9ble 9, France
Citazione:
M.L. Grattone et al., "Co-operation between human CR1 (CD35) and CR2 (CD21) in internalization oftheir C3b and iC3b ligands by murine-transfected fibroblasts", IMMUNOLOGY, 98(1), 1999, pp. 152-157

Abstract

CR1 and CR2 are expressed as associated proteins on the B-lymphocyte surface. To investigate their respective contributions to the internalization ofC3 fragments, transfected murine fibroblasts expressing human CR1, CR2, orboth CR1 and CR2 were produced. CR1- and CR1-CR2-expressing cells bound C3b and C3b-dimer whereas CR2- and CR1-CR2-expressing cells bound iC3b and C3de. In all cases, maximum binding was achieved at low ionic strength. CR1-CR2-positive cells internalized two- to threefold more C3b and 1.5-fold moreiC3b than CR1- and CR2-single-positive cells, respectively. Internalization of the anti-CR1 antibody J3D3, or C3de was at the same level, in both double-transfected and single-transfected cells. Furthermore, the internalization of C3b dimer by CR1-CR2 cells was impaired in the presence of OKB7, an anti-CR2-blocking antibody, but it was not altered in CR1 cells. Taken together, these findings suggest that CR1 and CR2 collaborate to internalize C3b and iC3b proteins. We suggest that the induction of conformational changes of the ligands enhances their binding to both receptors.

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Documento generato il 01/12/20 alle ore 01:12:16